Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP831079.RAD9EC3WQUDIs51C4e5ei9RFnUWCq66DGP2Vk5KsPRfDM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP831079.RAD9EC3WQUDIs51C4e5ei9RFnUWCq66DGP2Vk5KsPRfDM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831079.RAD9EC3WQUDIs51C4e5ei9RFnUWCq66DGP2Vk5KsPRfDM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831079.RAD9EC3WQUDIs51C4e5ei9RFnUWCq66DGP2Vk5KsPRfDM130_provenance.
- NP831079.RAD9EC3WQUDIs51C4e5ei9RFnUWCq66DGP2Vk5KsPRfDM130_assertion description "[We screened 19 patients with HSCR and mental retardation and eventually identified large-scale SMADIP1 deletions or truncating mutations in 8 of 19 patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831079.RAD9EC3WQUDIs51C4e5ei9RFnUWCq66DGP2Vk5KsPRfDM130_provenance.
- NP831079.RAD9EC3WQUDIs51C4e5ei9RFnUWCq66DGP2Vk5KsPRfDM130_assertion evidence source_evidence_literature NP831079.RAD9EC3WQUDIs51C4e5ei9RFnUWCq66DGP2Vk5KsPRfDM130_provenance.
- NP831079.RAD9EC3WQUDIs51C4e5ei9RFnUWCq66DGP2Vk5KsPRfDM130_assertion SIO_000772 11595972 NP831079.RAD9EC3WQUDIs51C4e5ei9RFnUWCq66DGP2Vk5KsPRfDM130_provenance.
- NP831079.RAD9EC3WQUDIs51C4e5ei9RFnUWCq66DGP2Vk5KsPRfDM130_assertion wasDerivedFrom befree-20150227 NP831079.RAD9EC3WQUDIs51C4e5ei9RFnUWCq66DGP2Vk5KsPRfDM130_provenance.
- NP831079.RAD9EC3WQUDIs51C4e5ei9RFnUWCq66DGP2Vk5KsPRfDM130_assertion wasGeneratedBy ECO_0000203 NP831079.RAD9EC3WQUDIs51C4e5ei9RFnUWCq66DGP2Vk5KsPRfDM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP831079.RAD9EC3WQUDIs51C4e5ei9RFnUWCq66DGP2Vk5KsPRfDM130_provenance.